bisoprolol fumarate and hydrochlorothiazide
- Product NDC
- 70934-705
- 11-digit product format
- 709340705
- Labeler code
- 70934
- Product ID
- 70934-705_a9ded063-8916-3001-e053-2a95a90a6d0c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bisoprolol fumarate and hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- ANDA079106
- Marketing category
- ANDA
- Marketing start
- 2020-05-13
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE; BISOPROLOL FUMARATE
- Active strength
- 6 mg/1; mg/1
- Pharmacologic classes
- Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS],Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70934-705-90 | bisoprolol fumarate and hydrochlorothiazide | 90 in 1 BOTTLE, PLASTIC | TABLET | 90 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70934-705 | BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE TABLET [DENTON PHARMA, INC. DBA NORTHWIND PHARMACEUTICALS] | 1 | Legacy NDC, 1 package rows | 20210814_a9decb0f-c07e-424c-e053-2995a90a5d49.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-705-90 | 70934070590 | 90 TABLET in 1 BOTTLE, PLASTIC (70934-705-90) | 90 tablet | 2020-05-13 | 0000-00-00 | No | No | Current |